Predicted mutation | |||||||
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evidence | seq id | position | mutation | freq | annotation | gene | description |
RA | NC_002947 | 4,042,376 | C→T | 19.0% | R140R (CGC→CGT) | PP_3563 → | hypothetical protein |
Read alignment evidence... | |||||||||||
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seq id | position | ref | new | freq | score (cons/poly) | reads | annotation | genes | product | ||
* | NC_002947 | 4,042,376 | 0 | C | T | 19.0% | 34.3 / 2.4 | 21 | R140R (CGC→CGT) | PP_3563 | hypothetical protein |
Reads supporting (aligned to +/- strand): ref base C (7/10); new base T (2/2); total (9/12) | |||||||||||
Fisher's exact test for biased strand distribution p-value = 1.00e+00 | |||||||||||
Kolmogorov-Smirnov test that lower quality scores support variant p-value = 9.14e-01 |
ACGCGCCGCCATGCATGCCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCGGGGTCGCCGCCAACCACA > NC_002947/4042244‑4042524 | acgcGCCGCCATGCATGCCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGc < 1:298382/150‑1 (MQ=255) gccgccATGCATGCCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAg < 2:450998/150‑1 (MQ=255) ccgccATGCATGCCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAgg < 1:523199/150‑1 (MQ=255) gcatgcCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGaa < 1:452768/150‑1 (MQ=255) catgcCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAg < 2:536335/150‑1 (MQ=255) aGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGGCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCagg > 2:112077/1‑150 (MQ=255) ttCTGCCAGGTGGTGCTCGACCCGCAATTCGTAGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAAc > 1:63359/1‑150 (MQ=255) gtcgATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGc > 2:984/1‑89 (MQ=255) gtcgATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGc < 1:984/89‑1 (MQ=255) atatCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGACACGGCAATGCGGCGGcc > 2:34291/1‑150 (MQ=255) aGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTgcc < 2:161705/150‑1 (MQ=255) gCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGTGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGccgccccgc < 2:217784/150‑1 (MQ=255) gcgcATCGTGCTGGCACGGCCCCTGCTCAGCGGCCCCCTGGGCAACTGGCAGGCCGAGGAACAGAAGGTCCTGCAGGAGTTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTg < 2:63359/150‑1 (MQ=255) aTCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGc > 2:220499/1‑150 (MQ=255) caggcGGCCGCTGAGCAGCGGCCGTCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCt > 1:9439/5‑150 (MQ=255) aggcGGCCGCTGAGCAGCGGCCGTCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCaggag < 1:206740/63‑1 (MQ=25) aggcGGCCGCTGAGCAGCGGCCGTCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCaggag > 2:206740/4‑66 (MQ=25) ccGCGGCTCACGGGCCGCCTGGGCGACTGGCAGGCCGGGGGACAGAAGGTGCTGAAGGAGGCCACCGCCGCGCGCAAGGTGCCACGGTAGTGGGGCGGCCCGCCTTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCggg < 2:455860/150‑1 (MQ=255) gctgctCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCGGGGt > 2:137783/1‑150 (MQ=255) ggctcccTGGGCGACCTGCAGCACGAGGAAGAAAGGGCGCTGCAGGAGGTCAACGCCGCGCGAAAGGTCCCAAGGCAATGCGGCGGCCGGACGTTGGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCGGGCCGGGGTCGCCGCCAAc < 1:220499/145‑1 (MQ=255) ggCCGTCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCGGGGTCGCCGCCAAc < 2:9439/150‑1 (MQ=255) ggCCGCCTTGGCGACTGGCAGGCCGAGGGACAGAAGGTGAGGCAGGAGGTCAACGCGGAGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCGGGGTCGCCGCCAAc > 2:178530/1‑150 (MQ=255) ccgccTGGGCGACGGGCAGGCCGAGGGACAGAAGGTGCGGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGTGGTTTGCCCCCGCCCCGCCACTAAGCTGGAGCGCAGTTCTGGCCGGGGTCGCCGCCAACca < 1:420604/150‑1 (MQ=255) gccTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCGGGGTCGCCGCCAACcaca > 2:539922/1‑150 (MQ=255) | ACGCGCCGCCATGCATGCCATCGAGGAAAGCTTCTGCCAGGTGGTGCTCGACCCGCAATTCGTCGATATCGGCGTCAGCCAGGAGGGCCGCGACTGGCGCATCGTGCTGGCACGGCCGCTGCTCAGCGGCCGCCTGGGCGACTGGCAGGCCGAGGGACAGAAGGTGCTGCAGGAGGTCAACGCCGCGCGCAAGGTGCCACGGCAATGCGGCGGCCAGCCGTTTGCCGCCGCCCCGCCACTAAGCTGGAGCACAGTGCTGGCCGGGGTCGCCGCCAACCACA > NC_002947/4042244‑4042524 |
Alignment Legend |
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Aligned base mismatch/match (shaded by quality score): ATCG/ATCG < 3 ≤ ATCG/ATCG < 12 ≤ ATCG/ATCG < 22 ≤ ATCG/ATCG < 37 ≤ ATCG/ATCG < 41 ≤ ATCG/ATCG |
Unaligned base: atcg Masked matching base: atcg Alignment gap: ‑ Deleted base: ‑ |